Fractional order differential equations for chronic liver cirrhosis with frequent hospitalization

Lemesa Bedjisa Dano1, Koya Purnachandra Rao2, Temesgen Duressa Keno2

  • 1Department of Mathematics, Wollega University, Nekemte, Ethiopia. lemesabjsa@gmail.com.

BMC Research Notes
|October 23, 2022
PubMed

Insights

This study models chronic liver cirrhosis dynamics using fractional differential equations. Mathematical analysis and simulations show that considering progression rate and past disease states can decrease decompensated cirrhosis cases.

Area of Science:

  • Mathematical modeling
  • Hepatology
  • Non-communicable diseases

Background:

  • Liver cirrhosis is a life-threatening, terminal stage of liver disease, often linked to viral hepatitis (B and C).
  • Cirrhosis progresses from asymptomatic compensated to symptomatic decompensated stages, marked by multi-systemic complications and hospitalization.
  • Understanding the dynamics of chronic liver cirrhosis is crucial for managing this global non-communicable disease.

Purpose of the Study:

  • To formulate a system of fractional differential equations for chronic liver cirrhosis, incorporating frequent hospitalizations.
  • To investigate the disease dynamics and analyze fundamental properties like solution existence and biological feasibility.
  • To develop and apply a numerical scheme for simulating the fractional order model.

Main Methods:

  • Formulation of a fractional differential equation system to model chronic liver cirrhosis.
  • Application of the generalized mean value theorem to establish the existence of positive solutions.
  • Implementation of an Adams-type predictor-evaluate-corrector-evaluate approach for numerical simulations using MATLAB.

Main Results:

  • Numerical simulations successfully illustrated the analytic findings of the fractional order model.
  • The analysis indicated a reduction in decompensated cirrhosis cases when progression rate and past disease states are considered.
  • The study confirmed the existence of positive solutions and the biological feasibility of the model.

Conclusions:

  • Fractional differential equations provide a valuable framework for modeling complex diseases like chronic liver cirrhosis.
  • The findings suggest that incorporating disease progression rates and historical data into models can inform strategies to reduce decompensated cases.
  • The developed numerical scheme is effective for simulating and analyzing fractional order models in disease dynamics.
Abstract

Related Concept Videos

Parameters Affecting Nonlinear Elimination: Zero-Order Input, First-Order Absorption and Two-Compartment Model01:13

Parameters Affecting Nonlinear Elimination: Zero-Order Input, First-Order Absorption and Two-Compartment Model

Drugs administered through various routes can lead to nonlinear elimination, resulting in complex pharmacokinetic behaviors crucial to understanding efficacious drug dosing.
When a drug is administered through a constant intravenous infusion and eliminated via nonlinear pharmacokinetics, it follows zero-order input. For example, oral drugs undergo first-order absorption upon administration and are eliminated through nonlinear pharmacokinetics.
In the case of subcutaneously administered drugs,...
116
Renal Failure: Dose Adjustments01:11

Renal Failure: Dose Adjustments

In patients with renal impairment, drugs undergo significant changes in their pharmacokinetics, which require dosage adjustments to ensure safe and effective therapy.
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
However, dosage adjustments...
141
Second Order systems II01:18

Second Order systems II

In an underdamped second-order system, where the damping ratio ζ is between 0 and 1, a unit-step input results in a transfer function that, when transformed using the inverse Laplace method, reveals the output response. The output exhibits a damped sinusoidal oscillation, and the difference between the input and output is termed the error signal. This error signal also demonstrates damped oscillatory behavior. Eventually, as the system reaches a steady state, the error diminishes to zero.
147
Compartment Models: Two-Compartment Model01:20

Compartment Models: Two-Compartment Model

The two-compartment model divides the body into central and peripheral compartments to account for varying blood perfusion rates among organs and tissues, affecting drug distribution. The central compartment includes blood and highly perfused tissues with rapid drug distribution, while the peripheral compartment contains tissues with slower drug distribution. After a single IV bolus dose, the drug concentration is high in plasma and low in tissues. The drug distribution between compartments...
5.8K
Three-Compartment Open Model01:06

Three-Compartment Open Model

The three-compartment open model is a pharmacokinetic model used to describe the distribution and elimination of drugs following extravascular administration. It comprises a central compartment representing the plasma and two peripheral compartments. The highly perfused peripheral compartment represents organs and tissues with a rich blood supply, such as the liver, kidneys, and lungs. The scarcely perfused peripheral compartment represents tissues with lower blood supply, such as adipose...
367
Hepatic Drug Excretion: Enterohepatic Cycling01:17

Hepatic Drug Excretion: Enterohepatic Cycling

Enterohepatic cycling involves the active secretion of drugs and their metabolites into the bile via transporters in the canalicular membrane of hepatocytes. This secretion is an integral part of the digestive process, releasing these substances into the gastrointestinal (GI) tract.
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...
1.7K